Team:UT-Tokyo/Miniprep
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*2. centrifuge for 10min (15,000rpm) | *2. centrifuge for 10min (15,000rpm) | ||
*3. throw supernatant fluid away not to damage the precipitation | *3. throw supernatant fluid away not to damage the precipitation | ||
- | ( you should decant by using yellow tip first / remove culture medium as you can / | + | **( you should decant by using yellow tip first / remove culture medium as you can / |
throw waste water away in bio hazard!) | throw waste water away in bio hazard!) | ||
*4. add 250μl cell resuspension solution (<font color="red">red label</font>)、suspend completely | *4. add 250μl cell resuspension solution (<font color="red">red label</font>)、suspend completely | ||
- | (incomplete suspending decreases yields / you should use epp stand like a washboard) | + | **(incomplete suspending decreases yields / you should use epp stand like a washboard) |
*5. add 250μl Cell lysis solution(<font color="green">green label</font>) | *5. add 250μl Cell lysis solution(<font color="green">green label</font>) | ||
*6. turn the tube upside down four times slowly not to bubble | *6. turn the tube upside down four times slowly not to bubble | ||
Line 35: | Line 35: | ||
*18. change the column into 1.5ml tube and centrifuge for 2min (15,000rpm) | *18. change the column into 1.5ml tube and centrifuge for 2min (15,000rpm) | ||
*19. change the tube into new one and add 50μl MilliQ | *19. change the tube into new one and add 50μl MilliQ | ||
- | (use Nucleas-Free Water in the kit instead of MilliQ) | + | **(use Nucleas-Free Water in the kit instead of MilliQ) |
*20. centrifuge for 1min (15,000rpm) after waiting for 1min | *20. centrifuge for 1min (15,000rpm) after waiting for 1min | ||
*21. take 1 to 1.5μl and determine the concentration by NanoDrop (Don’t dilute) | *21. take 1 to 1.5μl and determine the concentration by NanoDrop (Don’t dilute) |
Latest revision as of 08:20, 23 September 2010
Miniprep
Preparation
- kit of Promega (SVMinipreps)
- incubative tube
- 2ml epp tube
- 1.5ml epp tube
- MilliQ
Procedure
- 1. pour contents out of the incubative tube into the 1.5ml tube as you can
- 2. centrifuge for 10min (15,000rpm)
- 3. throw supernatant fluid away not to damage the precipitation
- ( you should decant by using yellow tip first / remove culture medium as you can /
throw waste water away in bio hazard!)
- 4. add 250μl cell resuspension solution (red label)、suspend completely
- (incomplete suspending decreases yields / you should use epp stand like a washboard)
- 5. add 250μl Cell lysis solution(green label)
- 6. turn the tube upside down four times slowly not to bubble
- 7. add 10μl Alkalin Protease Sol. (small bottle)
- 8. turn the tube upside down four times slowly not to bubble
- 9. wait for 5min (Be careful not to exceed 5min! colon bacillus will disintegrate too much!)
- 10. add 350μl Neutralization Sol. (blue label)
- 11. turn the tube upside down four times slowly not to bubble
- 12. centrifuge for 10min (15,000rpm)
- 13. put the supernatant fluid to column (germ’s wreckage is adhering below)
- 14. centrifuge for 1min (15,000rpm)
- 15. throw flow through (the liquid in the tube below) away
- 16. add 750μl Wash Sol. to column and centrifuge for 1min (15,000rpm)
- 17. throw flow through away, put 250μl Wash Sol. to column and centrifuge for 1min (15,000rpm)
- 18. change the column into 1.5ml tube and centrifuge for 2min (15,000rpm)
- 19. change the tube into new one and add 50μl MilliQ
- (use Nucleas-Free Water in the kit instead of MilliQ)
- 20. centrifuge for 1min (15,000rpm) after waiting for 1min
- 21. take 1 to 1.5μl and determine the concentration by NanoDrop (Don’t dilute)
- 22. label them
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